Gene: NDUFA9 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4704
Gene Symbol: NDUFA9
NDUFA9 		0.300 Biomarker disease CLINGEN NDUFA9 point mutations cause a variable mitochondrial complex I assembly defect. 28671271 2018
Entrez Id: 4704
Gene Symbol: NDUFA9
NDUFA9 		0.300 Biomarker disease CLINGEN Structure of mammalian respiratory complex I. 27509854 2016
Entrez Id: 4704
Gene Symbol: NDUFA9
NDUFA9 		0.300 Biomarker disease CLINGEN Proteomics. Tissue-based map of the human proteome. 25613900 2015
Entrez Id: 4704
Gene Symbol: NDUFA9
NDUFA9 		0.300 Biomarker disease CLINGEN Gene knockout using transcription activator-like effector nucleases (TALENs) reveals that human NDUFA9 protein is essential for stabilizing the junction between membrane and matrix arms of complex I. 23223238 2013
Entrez Id: 4704
Gene Symbol: NDUFA9
NDUFA9 		0.300 Biomarker disease CLINGEN Defective NDUFA9 as a novel cause of neonatally fatal complex I disease. 22114105 2012